A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15203638



Internal ID5205454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30628576..30700028hg38UCSC Ensembl
chr15:30920779..30992231hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3871453
hg1971453
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636025
Supporting Variants
SamplesNA18960
Known GenesARHGAP11B, LOC100288637
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15203638
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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